RecruitingNCT06298565
A Non-interventional, Post-authorisation Safety Study of Patients Treated With Efgartigimod Alfa
Studying Adult-onset myasthenia gravis
Last synced from ClinicalTrials.gov
ℹ
Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- argenx
- Intervention
- efgartigimod(biological)
- Enrollment
- 680 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2024 – 2034
Study locations (30)
- UCSF Medical Center - Helen Diller Family Comprehensive Cancer Center - Brain Tumor Center,, San Francisco, California, United States
- SFM Clinical Research, LLC, Boca Raton, Florida, United States
- University of Florida College of Medicine Jacksonville, Jacksonville Beach, Florida, United States
- Medsol Clinical Research Center Inc, Port Charlotte, Florida, United States
- BayCare Health System, Inc. St Anthony's Hospital, St. Petersburg, Florida, United States
- Prairie Education and Research Cooperative and HSHS Medical Group, O'Fallon, Illinois, United States
- University of Iowa, Iowa City, Iowa, United States
- University of Kansas Medical Center, Kansas City, Kansas, United States
- Norton Neuroscience Institute, Louisville, Kentucky, United States
- Massachusetts General Hospital, Boston, Massachusetts, United States
- Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States
- Henry Ford Health System, Detroit, Michigan, United States
- Oregon Health and Science University, Portland, Oregon, United States
- University of Colorado Hospital, Portland, Oregon, United States
- Medical University of South Carolina, Charleston, South Carolina, United States
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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